Uneeg Medical A/S is one of 94 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Uneeg Medical A/S - FDA 510(k) Cleared Devices
Recent clearances: UNEEG EpiSight System
1
Total
1
Cleared
0
Denied
Uneeg Medical A/S has 1 FDA 510(k) cleared medical devices. Based in Alleroed, DK.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Uneeg Medical A/S Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Uneeg Medical A/S
1 devices